4 results on '"Zhimiao Lin"'
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2. Progressive symmetric erythrokeratodermia with spinocerebellar ataxia due to ELOVL4 mutation in a Chinese family
3. Late-onset hereditary sensory and autonomic neuropathy type 2B caused by novel compound heterozygous mutations in FAM134B presenting as chronic recurrent ulcers on the soles
4. Tonsillar fat herniation: A novel finding in Goltz syndrome
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